The evolution of the clinical trial ancillary supply chain (CTASC), the globalisation and expansion of clinical trials in the most difficult regions of the world, and the requirement for better, faster and leaner methods, have presented a myriad of unforeseen and unprecedented risks and challenges for the CTASC organisation. The CTASC professional must possess the ability to research, evaluate, execute and guarantee that all components and all links in the chain align to achieve success.
As published in International Clinical Trials: Clinical Trial Supply and Logistics Supplement
